Methylation reactions play an important role in the transformation of
endogenous and exogenous substances. Up to 85% of all transmethylation
reactions occur in the liver. Several studies have shown that these m
etabolic processes are greatly influenced by the presence of hepatic d
iseases. We investigated the methylation of nicotinamide in 16 control
subjects and in 29 patients with cirrhosis (19 Child A, 10 Child B).
The basal serum value of N-methyl-nicotinamide was measured in all sub
jects. In seven controls and in nine patients with cirrhosis (5 Child
A and 4 Child B), the serum levels and urinary excretion (5 and 24 h)
of N-methyl-nicotinamide were also evaluated after oral administration
of nicotinamide (1.5 mg/kg body weight). The basal serum levels of N-
methyl-nicotinamide were significantly (p<0.05) higher in patients wit
h cirrhosis (Child A: median 34 ng/ml, 16th percentile 24, 84th percen
tile 61; Child B median 45, 16th percentile 34, 84th percentile 81) th
an in controls (median 22, 16th percentile 13, 85th percentile 28). Af
ter the nicotinamide load the urinary excretion and the time course of
serum N-methyl-nicotinamide in cirrhosis were also higher (p<0.05) th
an in controls (24 h urinary excretion=66.2 mg+/-5 S.D. in cirrhosis;
47.2+/-10.3 in controls) (area under the serum concentration versus ti
me curve=68 mu g.ml(-1) min(-1)+/-22 S.D. in cirrhosis; 32+/-15 in con
trols). In conclusion, our results show that cirrhosis does not impair
the efficiency of nicotinamide methylation. (C) Journal of Hepatology
.